Vasmed Technologies

Designed for precision, performance, and
reliability in complex PCI

Vas Track semi-compliant workhorse balloon catheter is engineered to deliver exceptional pushability, trackability, and crossability, making it ideal for challenging coronary interventions. Specifically designed for pre-dilation in de novo and restenotic lesions, as well as for normal balloon angioplasty.

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Superior Crossability & Trackability:

A combination of low-profile tip design, optimized shaft construction, and hydrophilic coating enable smooth navigation through tortuous anatomy, enhances push force transmission, ensuring reliable lesion access.
Enhanced Procedural Control

The unique stainless steel hypo tube construction ensures outstanding torque response, push ability, and trackability, giving the operator precise control from the guide catheter to the lesion.
High Pressure Dilation

Semi-complaint balloon with lowered wall thickness enables better adaptation to the structure of lesions without compromising safety, and provides controlled expansion with balanced compliance. Controlled expansion up to a Rated Burst Pressure (RPB) of 16 atm.
Superior Visibility

Dual platinum-iridium marker bands offer excellent radiopacity for clear, unambiguous positioning under fluoroscopy.

Technical Specifications

Catheter Type	Rapid Exchange RX
Compliance Type	Semi-Compliant
Balloon Folding	Tri-Fold
Total Working Length	142cm
Balloon Lengths (in mm)	10 mm – 42 mm (10, 15, 20, 25, 30, 32,34, 36 ,38 and 42 mm)
Balloon Diameters (in mm)	1 mm – 4.0 mm (1.00, 1.25, 1.50, 2.00, 2.50,2.75, 3.00 ,3.25, 3.50, 3.75)
Distal Shaft Diameter	2.3 Fr (1.00 to 2.00mm) 2.6 Fr (2.50 to 4.00mm)
Proximal Shaft Diameter	1.9 Fr
Balloon Nominal Pressure (N/P)	8 atm
Balloon Rated Burst Pressure (RBP)	16 atm
Balloon Crossing Profile:	1.00 to 1.25 mm ≤ 0.024” (≤ 0.5842mm) 1.50 – 2.00 mm ≤ 0.025” (≤ 0.635 mm) 2.50 – 3.00 mm ≤ 0.030” (≤ 0.762 mm) 3.25 – 3.50 mm ≤ 0.031” (≤ 0.787 mm) 3.75 mm ≤ 0.034” (≤ 0.864 mm) 4.00 mm ≤ 0.036” (≤ 0.914 mm)

Balloon Material	Nylon
Marker Material	Platinum-Iridium
Radiopaque Markers
Single Marker & Double Markers	1.0mm to 2.0mm
Double Markers	2.5 to 4.00 mm
Tip Length	4mm
Tip Entry Profile	0.019”
Distal Coating	Hydrophilic
Minimum Guiding Catheter ID	5 Fr
Maximum Guide Wire Compatibility	0.014”
Inflation Time	<10 sec
Deflation Time	<25 sec
Shelf Life	36 months

Compliance Chart

This chart illustrates the non-compliant nature of the Vastrack balloon, showing minimal diameter growth from Nominal to Rated Burst Pressure, ensuring predictable and controlled dilation

Size	4atm	6atm	8atm	10atm	12atm	14atm	16atm	18atm	20atm
1.00mm	0.84	0.92	0.97	1.01	1.03	1.10	1.15	1.23	1.33
1.25mm	1.01	1.10	1.16	1.25	1.33	1.43	1.54	1.65	1.79
1.50mm	1.30	1.43	1.52	1.59	1.66	1.72	1.77	1.82	1.87
2.00mm	1.68	1.83	1.95	2.04	2.11	2.17	2.22	2.28	2.32
2.50mm	2.08	2.30	2.46	2.52	2.57	2.61	2.66	2.71	2.77
2.75mm	2.38	2.61	2.72	2.79	2.85	2.91	2.97	3.02	3.09
3.00mm	2.62	2.83	2.97	3.06	3.13	3.19	3.25	3.32	3.39
3.25mm	2.95	3.11	3.22	3.29	3.36	3.42	3.46	3.52	3.58
3.50mm	3.13	3.33	3.46	3.53	3.58	3.65	3.71	3.78	3.85
3.75mm	3.30	3.53	3.72	3.78	3.84	3.90	3.96	4.00	4.07
4.00mm	3.57	3.77	3.97	4.05	4.12	4.20	4.27	4.34	4.41
Nominal Pressure						Rated Burst Pressure

Warnings & Safety

The VasTrack Balloon catheters are indicated as post dilatation catheters for the post-delivery expansion of balloon expandable stents (Bare Metal & Drug Eluting Stents) during the PCI procedures.

The VasTrack Balloon catheters are intended for use in patients with the symptomatic ischemic heart disease due to discrete denovo or restenotic lesions with reference vessel diameter of 2.50 mm to 4.00mm and length ≤ 30mm, for the purpose of post-delivery expansion of balloon expandable stents during the Percutaneous Transluminal Coronary.

Possible adverse effects include, but are not limited to, the following:

Artery spasm
Dissection, rupture, perforation or injury of arteries which may require vessel repair
Hypo/hypertension
Ischaemia or acute myocardial infarction
Ventricular fibrillation and flutter
Unstable angina, palpitation
Re-stenosis or total occlusion of the dilated artery
Vascular or stent thrombosis or embolism, distal emboli.
Haemorrhage haematoma and/or haematuria and/or haemoptysis
Pseudoaneurysm
Infection, inflammation and/or fever
Cardiac arrhythmia, extra systoles, bradycardia and tachycardia
Conduction disturbance
Arteriovenous fistula
Allergic reactions to stent materials, contrast medium or other drug reactions
Death
Access site complications
Please also consider the latest medical research findings.

Patients who are unsuitable for bypass surgery and/or PTCA
Patients who are unsuitable for treatment with the necessary medication (eg. anticoagulants, antiplatelet therapy).
Imminent thrombus formation and alteration of flow after myocardial infarction.
Evidence of existing thrombus.
Severe allergic reactions to contrast medium
Treatment of an unprotected left main coronary artery lesion, of proximal lesions, or of significant vessel tortuosity which prohibits guide wire access and sufficient guiding catheter support
Patients in whom insufficient predilatation of the lesion is possible
Spasm of the arteries in absence of stenosis or previously diagnosed severe coronary-arterial or arterial spasms
Please also consider the latest medical research findings.
This device is not intended to use for children and pregnant women.

NOT use the balloon catheter if the sterile package is damaged or after the sterility expiry date.
Balloon expansion must always be performed under high quality fluoroscopic control.
This device is provided sterile and is intended for single patient use only. DO NOT re-sterilize. DO NOT re-use.
This device should only be used by trained physicians experienced in Percutanious Transluminal Coronary Angioplasty (PTCA) and coronary stenting techniques.
Always open the haemostatic valve fully before feeding the catheter through it.
If resistance is met during advancement or manipulation of the catheter system, determine the cause of the resistance before proceeding.
The High Track Rapid Exchange PTCA Balloon Catheter Low Compliant High Burst Pressure is not designed for use in CTO or >90% occlusions due to the large profile of the balloon.
Never forcibly advance the balloon catheter.
Use appropriate balloon inflation medium – do not use any gaseous medium or air to inflate the balloon. Do not exceed the rated balloon burst pressures. Refer to compliance chart for guidance.
Should the risk of embolisation necessitate removal of the catheter prior to expansion, the guiding catheter and PTCA catheter should be removed as one unit.
If the balloon gets caught and is unable to be removed by normal means, it should be removed via cardiac surgery.
A cardiac surgery team must always be on stand-by during stent implantation procedures so that emergency coronary bypass surgery can be quickly performed in the event of potential injuries or life threatening complications.
After use, this product may be contaminated and should be disposed using standard hospital practice.
The device is not intended to use for children and pregnant women without prior consultation of pediatrician / obstetrician.

Vas Track

Designed for precision, performance, and reliability in complex PCI

Technical Specifications

Compliance Chart

Warnings & Safety

Indications for use

Intended purpose

Adverse effects

Contra-indications

Warnings

Designed for precision, performance, and
reliability in complex PCI